✦ LIBER ✦

Abnormal platelet von willebrand factor interaction in patients with TTP

✍ Scribed by Dr. G. Rock; P. Tittley; J. R. Taylor

Publisher: John Wiley and Sons
Year: 1988
Tongue: English
Weight: 484 KB
Volume: 27
Category: Article
ISSN: 0361-8609
DOI: 10.1002/ajh.2830270306

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Platelet von willebrand factor abnormali

Platelet von willebrand factor abnormalities in myeloproliferative syndromes

✍ Dr. Giancarlo Castaman; Antonella Lattuada; Marco Ruggeri; Alberto Tosetto; Pier 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 496 KB 👁 1 views

Abnormal platelet von willebrand factor

Abnormal platelet von willebrand factor (vWF) as a marker of abnormal function in megakaryocytic dysplasia

✍ F. de Cataldo; F. Baudo; R. Redaelli; A. R. Corno 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 475 KB 👁 1 views

Multimeric pattern of plasma and platele

Multimeric pattern of plasma and platelet von willebrand factor is normal in uremic patients

✍ Giancarlo Castaman; Dr. Francesco Rodeghiero; Antonella Lattuada; Giuseppe La Gr 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 English ⚖ 387 KB 👁 1 views

Increased von willebrand factor antigen

Increased von willebrand factor antigen in the plasma of patients with vasculitis

✍ Steven R. Nusinow; Augusto B. Federici; Theodore S. Zimmerman; John G. Curd 📂 Article 📅 1984 🏛 John Wiley and Sons 🌐 English ⚖ 445 KB 👁 1 views

The plasma concentrations of von Willebrand factor antigen (vWF:Ag) were determined in 101 patients who had the following diagnoses: vasculitis 8 patients, systemic lupus erythematosus (SLE) 51, rheumatoid arthritis (RA) 28, asthma 7, hereditary angioedema 7. The greatest mean concentration of vWF:A

Giant platelet disorder in a patient wit

Giant platelet disorder in a patient with type 2B von Willebrand's disease

✍ Moll, Stephan; Lazarowski, Alicia Rico; White, Gilbert C. 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 292 KB 👁 1 views

While patients with type 2B von Willebrand's disease often exhibit thrombocytopenia, platelet morphology is typically normal. We describe a 44-year-old Jamaican man with thrombocytopenia and a history of bleeding, who had giant platelets on his peripheral blood film. Functional studies and von Wille

Increased von Willebrand factor (vWf) bi

Increased von Willebrand factor (vWf) binding to platelets associated with impaired vWf breakdown in thrombotic thrombocytopenic purpura

✍ Joel L. Moake; Thomas W. Chow 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 220 KB 👁 1 views

Thrombotic thrombocytopenic purpura (TTP) is a disorder of systemic platelet aggregation. Evidence has accumulated that the aggregating agonist in TTP of all types is likely to be von Willebrand factor (vWf), especially unusually large vWf multimers derived from endothelial cells. Recent evidence in